EP0459387A2 - Test für Phencyclidin und Phencyclidin-Metaboliten, Tracer, Immunogene, Antikörper und Reagenzsatz dafür - Google Patents

Test für Phencyclidin und Phencyclidin-Metaboliten, Tracer, Immunogene, Antikörper und Reagenzsatz dafür Download PDF

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EP0459387A2
EP0459387A2 EP19910108674 EP91108674A EP0459387A2 EP 0459387 A2 EP0459387 A2 EP 0459387A2 EP 19910108674 EP19910108674 EP 19910108674 EP 91108674 A EP91108674 A EP 91108674A EP 0459387 A2 EP0459387 A2 EP 0459387A2
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Prior art keywords
phencyclidine
tracer
compound
antibodies
assay
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French (fr)
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EP0459387B1 (de
EP0459387A3 (en
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Robert Edward Dubler
Mary Pat Frintner
Jonathan Grote
David James Hawksworth
Daniel S. Nam
Larry Kay Wray
Gregg Allen Hadley
Hal Dayton Hopkins
Frank S. Ungemach
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Abbott Laboratories
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Abbott Laboratories
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K17/00—Carrier-bound or immobilised peptides; Preparation thereof
    • C07K17/02—Peptides being immobilised on, or in, an organic carrier
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/94—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving narcotics or drugs or pharmaceuticals, neurotransmitters or associated receptors
    • G01N33/9486—Analgesics, e.g. opiates, aspirine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40—Oxygen atoms
    • C07D211/44—Oxygen atoms attached in position 4
    • C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D211/74—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
    • C07D295/033—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/155—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/44—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material not provided for elsewhere, e.g. haptens, metals, DNA, RNA, amino acids
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/58—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances
    • G01N33/582—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances with fluorescent label
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S436/00—Chemistry: analytical and immunological testing
    • Y10S436/815—Test for named compound or class of compounds
    • Y10S436/816—Alkaloids, amphetamines, and barbiturates
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
    • Y10S530/807—Hapten conjugated with peptide or protein

Definitions

  • the present invention relates to a method and reagents for performing a fluorescence polarization immunoassay (FPIA) to determine the presence or amount of phencyclidine and phencyclidine metabolites in samples, especially fluid biological samples such as urine, serum or plasma, to a method of making the reagents, and to an assay kit containing the reagents.
  • FPIA fluorescence polarization immunoassay
  • the invention relates particularly to (1) reagents (tracers and antibodies, and an assay kit containing the tracers and antibodies) for determining the presence or amount of phencyclidine and phencyclidine metabolites in a sample; (2) immunogen compounds used to raise monoclonal or polyclonal antibodies; (3) synthetic methods for making the tracer and immunogen compounds; and (4) analytical methods for conducting the assay.
  • Phencyclidine is a synthetic drug with potent analgesic and anesthetic properties. This drug has been shown to produce serious and prolonged post-anesthetic confusion and delirium. Its tendency to produce hallucinations, euphoria, distortions in perceptions, and feelings of dissociation have lead to illicit use and abuse. Recurring abuse has intensified efforts to prevent its manufacture and distribution. Consistent with these efforts, there exists a need for detection methods which are rapid, reliable and selective for phencyclidine and phencyclidine metabolites.
  • Phencyclidine is metabolized into two major metabolites, 4-phenyl-4-piperidinocyclohexanol and 1-(1-phenylcyclohexyl)-4-hydroxypiperidine, each of which is excreted mostly in the urine along with the corresponding glucuronide conjugates. Detection of either phencyclidine or phencyclidine metabolites indicates phencyclidine use.
  • Urine samples are non-invasive of the body, and are generally more accessible than blood samples. However, testing of other biological materials is also possible.
  • competitive binding immunoassays are used for measuring ligands in a test sample.
  • a "ligand” is a substance of biological interest to be quantitatively determined by a competitive binding immunoassay technique).
  • the ligands compete with a labeled reagent (a "ligand analog” or "tracer") for a limited number of ligand binding sites on antibodies specific to the ligand and ligand analog.
  • the concentration of ligand in the sample determines the amount of ligand analog which binds to the antibody, and the amount of ligand analog that will bind to the antibody is inversely proportional to the concentration of ligand in the sample, because the ligand and the ligand analog each bind to the antibody in proportion to their respective concentrations.
  • FPIA techniques provide a quantitative means for measuring the amount of tracer-antibody conjugate produced in a competitive binding immunoassay.
  • Such procedures are based on the principle that a fluorescent labeled compound, when excited by plane polarized light, will emit fluorescence having a degree of polarization inversely related to its rate of rotation. Accordingly, when a tracer-antibody conjugate having a fluorescent label is excited with plane polarized light, the emitted light remains highly polarized because the fluorophore is constrained from rotating between the time that light is absorbed and emitted. In contrast, when an unbound tracer is excited by plane polarized light, its rotation is much faster than the corresponding tracer-antibody conjugate and the molecules become more randomly oriented. As a result, the light emitted from the unbound tracer molecules is depolarized.
  • Riboflavin interference A problem that heretofore has prevented the accurate determination of phencyclidine and other "drugs of abuse" in urine by FPIA techniques is that of riboflavin interference.
  • Riboflavin, or vitamin B2 is a common constituent of many foods and of commercially available vitamin supplements. Riboflavin is excreted primarily in the urine and has a fluorescence spectrum quite similar to that of fluorescein. As a result, the presence of riboflavin in even moderate amounts in urine samples creates an interference which can produce erroneous data. While ordinary consumption of riboflavin is unlikely to produce more than trace amounts of riboflavin in the urine, test results can readily be distorted by the consumption of excessive quantities of vitamin supplements by persons wishing to prevent detection of phencyclidine.
  • the present invention offers an advance in the art in that tracers, a method for making the tracers, and an assay using the tracers and monoclonal or polyclonal antibodies are provided specifically for the determination of phencyclidines and phencyclidine metabolites without riboflavin interference.
  • the present invention is directed to a fluorescence polarization immunoassay for phencyclidine and phencyclidine metabolites; to tracers, immunogens and antibodies; to a reagent kit containing tracers and antibodies for use in the assay; and to methods for making the tracers, immunogens and antibodies.
  • a first aspect of the invention relates to the discovery of unique tracers and immunogens having novel structures.
  • the tracers and the immunogens can both be represented by each of the structural formulas shown in Figures 5 and 20 wherein: W is CH or N; R is a linking group including up to 4 heteroatoms, and having a total of from 0 to 8 carbon atoms and heteroatoms, arranged in a straight or branched chain, and containing up to one aliphatic or aromatic ring structure, said heteroatoms being O, N, S, P or F; Z is NH, CO, CNH, or OCO; n is 0 or 1 when W is N and n is 1 when W is CH; and Q is a poly(amino acid), a poly(amino acid) derivative, fluorescein or a fluorescein derivative.
  • the compound when Q is a poly(amino acid) or a derivative thereof, the compound can be used as an immunogen.
  • Q is fluorescein or a derivative thereof, the compound can be used as a tracer.
  • a second aspect of the invention relates to monoclonal or polyclonal, preferably monoclonal, antibodies raised against the novel immunogens of the invention.
  • monoclonal or polyclonal antibodies are prepared in response to a compound according to one of the aforementioned structural formulas ( Figures 5 or 20), when Q is a poly(amino acid) or a derivative thereof.
  • an immunogen is made by a method comprising the step of coupling a compound represented by either of the structural formulas shown in Figures 3 or 21, wherein: W is CH or N; R is a linking group including up to 4 heteratoms, and having a total of from 0 to 8 carbon atoms and heteroatoms, arranged in a straight or branched chain, and containing up to one aliphatic or aromatic ring structure, said heteroatoms being O, N, S, P or F; Z is NH2, COOH, CN, CHO or OH; and n is 0 or 1 when W is N and n is 1 when W is CH; with a poly(amino acid) or a derivative of a poly(amino acid).
  • a fifth aspect of the invention relates to the elimination of potential fluorescence interference by riboflavin.
  • Riboflavin binding protein (RBP) is added either directly to each sample, or to one or more of the reagents utilized in the assay, wherein it binds all riboflavin which may be present in the sample into RBP-riboflavin complexes, thus eliminating fluorescence interference.
  • RBP Riboflavin binding protein
  • Other fluorescence-quenching substances may also be utilized for this purpose.
  • a process for detecting or measuring the concentration of phencyclidine and phencyclidine metabolites is provided.
  • a sample is contacted with a phencyclidine derivative antiserum, and with a fluorescein-containing phencyclidine derivative capable of producing a detectable fluorescence polarization response to the presence of the phencyclidine derivative antiserum.
  • Plane polarized light is then passed through the solution to obtain a fluorescence polarization response, and this response is detected as a measure of the amount of phencyclidine and phencyclidine metabolite in the sample.
  • a seventh aspect of the present invention relates to a stabilized reagent kit which is useful for determining the presence or amount of phencyclidine and phencyclidine metabolites in a sample.
  • the reagent kit contains novel tracers, and salts thereof, which are useful as reagents in the novel method of the present invention.
  • reagent kit include: (1) a solution containing an amount of riboflavin binding protein which is effective to reduce fluorescence interference by riboflavin; (2) a monoclonal or polyclonal antibody reagent which has been raised against an immunogen which is capable of specifically recognizing and binding phencyclidine and phencyclidine metabolites and the novel tracer reagents of the present invention; and (3) a wash solution containing a sufficient amount of dimethylformamide and a sufficient amount of butanol to wash the probe of an automated or semiautomated instrument used to conduct the assay, with the result that carryover of phencyclidine from one sample to the next sample is reduced.
  • Figure 1 shows the structure of phencyclidine.
  • Figure 2 shows a class of reactants for a method of making a tracer in accordance with the present invention.
  • Figure 3 shows a class of reactants for a method of making an immunogen in accordance with the present invention.
  • Figure 4 shows the alternate structural formula and names of the fluorescein moiety included in the tracers of the present invention.
  • Figure 5 shows a general structural formula for the tracers and the immunogens of the present invention.
  • Figure 6 shows a general structural formula for the immunogens of the present invention.
  • Figure 7 shows a general structural formula for the tracers of the present invention.
  • Figure 8 shows a structural formula for preferred immunogens of the present invention.
  • Figure 9 shows a structural formula for preferred tracers of the present invention.
  • Figure 10 shows a precursor for the immunogens shown in Figures 6 and 8 and for the tracers shown in Figures 7 and 9.
  • Figure 11 shows various linkages that couple the fluorescein moiety to the precursor at the Z position in Figure 10, when Figure 10 represents a precursor for the tracers shown in Figures 7 and 9.
  • Figures 12 through 16 show various examples of structures of tracers in accordance with the present invention.
  • Figures 17 through 19 show various examples of structures of hapten reactants used to form the immunogens of the present invention.
  • Figure 20 shows another general structural formula for the tracers and the immunogens of the present invention.
  • Figure 21 shows a precursor for the immunogens and tracers of the present invention.
  • Figure 22 shows a structural formula for the most preferred immunogens of the present invention.
  • Figure 23 shows the structure of the most preferred immunogen of the present invention.
  • the present invention involves the use of fluorescein and derivatives of fluorescein.
  • a necessary property of fluorescein and its derivatives for the usefulness of the tracer compounds of the present invention is the fluorescence of fluorescein.
  • Fluorescein exists in two tautomeric forms, illustrated in Figure 4, depending on the acid concentration (pH) of the environment.
  • the open (acid form) there are a number of conjugated double bonds which make that form of fluorescein (and compounds containing a fluorescein moiety) capable of absorbing blue light and emitting green fluorescence after an excited state lifetime of about 4 nanoseconds.
  • the open and closed forms coexist, the relative concentration of molecules in the open and closed forms is easily altered by adjustment of the pH level.
  • the tracer compounds of the present invention exist in solution as biologically acceptable salts such as sodium, potassium, ammonium and the like, which allows the compounds to exist in the open, fluorescent form, when employed in the analytical methods of the present invention.
  • the specific salt present will depend on the buffer employed to adjust the pH level. For example, in the presence of a sodium phosphate buffer, the compounds of the present invention will generally exist in the open form, as a sodium salt.
  • fluorescein either as an individual compound or as a component of a larger compound, is meant to include both the open and closed forms, if they exist for a particular molecule, except in the context of fluorescence. An open form is necessary for the fluorescence to occur.
  • the numbering of carbon atoms of the fluorescein molecule varies, depending upon whether the open or closed form of the molecule is considered. Accordingly, the literature concerning fluorescein and its compounds is not uniform as to carbon atom numbering.
  • the para-carbon to the carbonyl of the lactone on the phenyl ring is numbered 6 (this is sometimes denominated "isomer II").
  • the para-carbon to the carboxylic acid group on the phenyl ring is numbered 5 (this is sometimes denominated "isomer I").
  • Figure 4 illustrates these isomers.
  • the numbering of the closed form is adopted because the raw materials used in the syntheses are most popularly numbered with that system.
  • the carbon atom of fluorescein and its compounds which is opposite the carboxyl group is therefore numbered "6" for the purposes of the present disclosure.
  • a tracer which is not complexed to an antibody is free to rotate in less than the time required for absorption and re-emission of fluorescent light.
  • the re-emitted light is relatively randomly oriented so that the fluorescence polarization of a tracer not complexed to an antibody is low, approaching zero.
  • the tracer-antibody complex thus formed assumes the rotation of the antibody molecule which is slower than that of the relatively smaller tracer molecule, thereby increasing the polarization observed. Therefore, when a ligand competes with the tracer for antibody sites, the observed polarization of fluorescence of the tracer-antibody complex becomes a value somewhere between that of the tracer and tracer-antibody complex.
  • the observed polarization value is closer to that of the free tracer, i.e., low. If the test sample contains a low concentration of the ligand, the polarization value is closer to that of the bound tracer, i.e., high.
  • Both the immunogens and the tracers of the present invention are represented by the general structural formulas described in the Summary of the Invention, and illustrated in Figures 5 and 20.
  • Q is a poly(amino acid)
  • the structure represents the immunogen
  • Q is a fluorescein derivative
  • the structure represents the tracer.
  • haptens are precursors of the immunogens, comprising generally a substituted phencyclidine derivative and a linking group to the poly(amino acid) carrier.
  • Suitable monoclonal or polyclonal antibodies can be produced from a variety of phencyclidine derivatives. Such antibodies are useful in a phencyclidine and phencyclidine metabolites assay according to the invention when combined with the appropriate tracer.
  • the immunogens of the present invention also have the general structural formulas shown in Figures 6, 8 and 22.
  • the immunogens have the structural formula shown in Figure 22.
  • the structure of the most preferred immunogen is shown in Figure 23.
  • thyroglobulin is the poly(amino acid) employed in the most preferred form of the immunogen of the present invention
  • various protein carriers may be employed, including albumins, serum proteins, e.g., globulins, ocular lens proteins, lipoproteins and the like.
  • Illustrative protein carriers include, in addition to thyroglobulin, bovine serum albumin, keyhole limpet hemocyanin, egg ovalbumin, bovine gamma-globulin, thyroxine binding globulin, etc.
  • synthetic poly(amino acids) may be prepared having a sufficient number of available amino groups, such as lysines, or carboxylic acid groups, such as glutamate.
  • the corresponding glutaraldehyde derivative of the above poly(amino acid) carriers may also be employed when the hapten coupling group is an amino group.
  • the immunogens can be prepared by coupling a compound of the class shown in Figure 3 or 21 with a poly(amino acid) or a derivative of a poly(amino acid), as will be discussed in the context of the synthetic method and the Examples below.
  • the possible variations in the structure of the tracers of the invention are even greater than the possible variations in the structure of the haptens thereof.
  • the tracers of the present invention have the general structural formulas described in the Summary of the Invention and illustrated in Figures 5 and 20, where Q represents a fluorescein moiety or a fluorescein derivative.
  • the phencyclidine or phencyclidine derivative can be attached to the fluorescein molecule or fluorescein derivative at any position on the fluorescein molecule or derivative at which the fluorescent properties of the molecule would be retained, including, as numbered in Figure 4 for the acid form of fluorescein, positions 4, 5 and 3a.
  • the tracers have the structural formula shown in Figure 9.
  • the tracers have the structure shown in Figure 14.
  • the tracer is a phencyclidine derivative which is linked to a fluorescein derivative by, e.g. , an amido, amidino, triazinylamino, carbamido, thiocarbamido, carbamoyl, thiocarbamoyl, or sulfomylcarbamoyl group, as shown in Figure 11.
  • the tracers are prepared by linking the appropriate fluorescein derivative to a phencyclidine derivative containing an amino, carboxylic acid, hydroxy, imidate, hydrazide, chloroformate, chlorothioformate, chlorosulfonyl-carbamoyl, isocyanate, thioisocyanate, or similar group, as will be discussed in the context of the synthetic method and the Examples below.
  • any of the following fluorescein derivatives can be used:
  • polyclonal and monoclonal antibodies recognize specific epitopes on an immunogen. Because polyclonal antibodies consist of a mixture of multiple antibodies, each recognizing a specific epitope, whereas monoclonal antibodies are produced by cells secreting a single antibody recognizing a specific epitope, and because monoclonal antibodies can be produced both in vitro and in vivo , monoclonal antibodies are the preferred antibodies for use in the method of the present invention, and for use in the reagent kit of the invention.
  • an assay of the invention which employs monoclonal antibodies is more desirous in that it: (1) results in a more selective assay; (2) results in an assay having a reduced interference with other compounds which may be present in the sample, and which may cross react with the antibodies and, thus, result in a number of falsely-positive readings for the presence of phencyclidine or phencyclidine metabolites when none was actually present in the sample; (3) eliminates the need for continued animal reimmunization and the labor-intensive process which is associated with such animal reimmunizations; and (4) eliminates the potential for irreproducibility of identical antiserum (because cross-reactive profiles of antibody-producing animals may change, requiring assay reconfiguration, because even carefully maintained animals can die, and because immunization of new animals may not result in the same cross reactivity profile as that originally produced).
  • monoclonal antibodies of the present invention may be prepared by injecting animals, such as mice or rats, intraperitoneally, subcutaneously, interveineously, or in some other manner, with an antigen (an immunogen, such as an immunogen having the structure shown in Figure 23) in order to elicit an immune response in the animals (the production of antibodies which are specific for the antigen).
  • an antigen an immunogen, such as an immunogen having the structure shown in Figure 23
  • Sera from the animals is then drawn, and the sera is tested to determine the titer of antibody in the sera (to determine whether or not the animal illicited the desired immune response, and to what extent).
  • Those animals in which the desired immune response has been produced are permitted to rest for approximately two to three months.
  • B-lymphocyte cells cells which, upon stimulation by antigen, mature into plasma cells which synthesize antibody, and which are also referred to as B cells
  • myeloma cells tumor cells
  • a boost injection of the antigen is administered to these animals.
  • B-lymphocyte cells are then removed from the spleens of these animals by standard procedures, and the B-lymphocyte cells are then fused with myeloma fusion partners according to standard procedures, such as those described in Kohler and Milstein, "Continuous Culture of Fused Cells Secreting Antibody of Predefined Specificity," Nature , 256, 495 (1975).
  • the B-lymphocyte-myeloma fusions are then plated in multiwell tissue culture plates containing HAT media, or other suitable media.
  • the resulting cultures are fed with HT media, or other suitable media, and fetal bovine serum or calf bovine serum on or about the fifth and seventh days after the fusion of the cells and then tested on or about the tenth day after the fusion for the presence of antibody which is specific for the antigen.
  • Specific desirable hybrids are then cloned by limiting dilution.
  • Hybrid cells are diluted in differing amounts of HT media, or other suitable media, and plated out in tissue culture plates in order to isolate a single desired clone.
  • Established clones are then retested for specificity to a broader panel of cross reactants.
  • the amount of the resulting monoclonal antibodies produced by a desired clone can then be scaled up to produce a sufficient quantity of antibody for purification in either: (1) tissue culture (by expanding the number of cells in tissue culture, or HT media); or (2) mice for ascites.
  • the monoclonal antibodies can be scaled up in mice by injecting hybrid cells into the abdominal cavity of mice and allowing the cells to grow (usually for about 7 days).
  • the ascites is harvested from the mice by sacrificing the mice, collecting the ascites fluid, and purifying the ascites fluid, as described in Example XVIII.
  • BALB/c mice are the most common strain of laboratory mouse used for this process, and they can be obtained from any mouse vendor, such as Jackson Laboratories, Bar Harbor, Maine, or Charles River, Willmington, Mass.
  • Pristane which may be obtained from Aldrich Chemical Co., Inc., Milwaukee, WI, should be injected into the mice in order to stimulate their immune systems to produce B and T cells (about two or three weeks before the hybrid cells are injected into the mice), which serve as a feeder layer for the clone cells that are injected into the mice. This is perfomed in order to provide a suitable environment in which the hybrid cells can grow.
  • Polyclonal antibodies of the present invention are prepared by developing a response in animals to the immunogens described above.
  • the immunogen is administered to animals such as rabbits or sheep by a series of injections, in a manner well-known to those skilled in the art.
  • the novel reagent kit of the present invention for determining the presence or amount of phencyclidine and phencyclidine derivatives in a sample comprises a salt of a first tracer of the formula shown in either Figure 5 or 20 wherein W, R, Z, n and Q are as defined in the Summary of Invention and monoclonal or polyclonal, preferably monoclonal, antibodies which have been raised against an immunogen having the structure shown in either Figure 5 or 20 wherein W, R, Z, n and Q are also as defined in the Summary of Invention.
  • the reagent kit will also contain an amount of riboflavin binding protein which is effective to reduce fluorescence interference by riboflavin and a wash solution containing dimethylformamide and butanol to wash the probe of an automated or semiautomated instrument used to conduct the assay.
  • riboflavin binding protein which is effective to reduce fluorescence interference by riboflavin
  • a wash solution containing dimethylformamide and butanol to wash the probe of an automated or semiautomated instrument used to conduct the assay.
  • the most preferred tracer for use in the reagent kit is a tracer having the structure shown in Figure 14
  • the most preferred antibodies for use in the kit are monoclonal antibodies generated against an immunogen having the structure shown in Figure 23.
  • the most preferred combination of tracer and antisera for use in the kit are the combination of a tracer having the structure shown in Figure 14 with monoclonal antibodies generated against an immunogen having the structure shown in Figure 23.
  • Both the immunogens and the tracers of the present invention can be made from a precursor having the general structural formula shown in Figures 2, 3, or 21 wherein: W is CH or N; R is a linking group including up to 4 heteroatoms, and having a total of from 0 to 8 carbon atoms and heteroatoms, arranged in a straight or branched chain, and containing up to one aliphatic or aromatic ring structure, said heteroatoms being O, N, S, P or F; Z is NH2, COOH, CN, CHO, or OH when the preparation is directed to an immunogen, and Z is NH2, COOH, CN, CHO, or OH, when the preparation is directed to a tracer; and n is 0 or 1 when W is N and n is 1 when W is CH.
  • the immunogens of the present invention are made by coupling a hapten, such as those having the general structure shown in Figures 2, 3 or 21 when Z is NH2, COOH, CN, CHO or OH, to a poly(amino acid).
  • the poly(amino acid) moiety can be linked to the hapten by an amide, an amidine, an alkyl, a urea, a thiourea, a carbamate, or a thiocarbamate linkage.
  • the hapten is preferably coupled under conditions normally used to form carbamate linkages, which conditions are well known to those skilled in the art. It is most preferred that pH conditions approximating pH 8.0 be used for forming the desired carbamate linkages, as these are the most effective for forming these linkages in this context.
  • the immunogens are prepared by coupling a hapten containing an -NH2, -CO2H, CONHNH2, -CNOR, -CHO, -NCO, -NCS, -OCOCl or -OCSCl group to a poly(amino acid).
  • the -NH2 case can be coupled by activating the carboxylic acid group on the poly(amino acid) in the presence of the -NH2 group.
  • the activation of the carboxylic acid groups on the poly(amino acid) can be accomplished by mixing the hapten and the poly(amino acid) with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC), N,N'-dicyclohexylcarbodiimide (DCC), 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate, or the like.
  • EDC 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide
  • DCC N,N'-dicyclohexylcarbodiimide
  • the -CO2H case is also coupled by the activation method (EDC) or the active este
  • the -CNOR case which is prepared from the corresponding cyano compound, is coupled directly to the poly(amino acid).
  • the -CHO case is coupled to the poly(amino acid) by reductive amination.
  • the poly(amino acid) is mixed with the -CHO hapten and the resulting imine is reduced with sodium cyanoborohydride to yield alkylated amines on the poly(amino acid).
  • the isocyanate (-NCO) and isothiocyanate (-NSC) cases which are prepared from the corresponding amino compound and chloroformate (-OCOCl) and chlorothioformate (-OCSCl) cases which are prepared from the corresponding alcohol compound, produce urea, thiourea, carbamate and thiocarbamate linkages, respectively. This is accomplished by direct coupling of the hapten to the poly(amino acid).
  • FIG. 21 shows an immunogen precursor class in accordance with a preferred embodiment of the method of the present invention.
  • the hapten is prepared by reaction of the appropriate piperidine derivative with cyclohexanone in the presence of cyanide.
  • the coupled product is then reacted with phenyl magnesium bromide to yield the hapten precursor.
  • the hapten precursor is then converted into the hapten.
  • benzyl can be used as a protecting group.
  • the benzyl group is removed after formation of the phencyclidine derivative.
  • This secondary amine is a suitable hapten. It is possible to alkylate the amine with an alkyl halide (Cl, Br or I), e.g. , bromoacetonitrile, 3-bromopropanol, 4-bromobutyric acid or the like, to prepare suitable haptens. It is also possible to form the chloroformamide derivative, which could make a suitable hapten, or form an amide derivative with an active ester, e.g.
  • the alcohol can be oxidized to the corresponding ketone which may be derivatized by known methods to a variety of compounds containing a suitable group useful for coupling to a carrier protein, e.g. , Wittig reagents, alkoxyamine compounds, reductive amination with amino compounds or the like. Reductive amination of the ketone with ammonium acetate results in an amino derivative.
  • the amino compound is suitable as a hapten or may be derivatized by known methods to a variety of hapten compounds analogous to the case where W is N and n is O.
  • Aldehydes and ketones can be condensed with (aminohydroxy)alkylcarboxylic acids, such as NH2OCH2CO2H, to produce substitued oxime derivatives.
  • the oxime alkyl carboxylic acid derivatives can be partially reduced to the corresponding (aminohydroxy)alkylcarboxylic acid derivatives.
  • the same type of condensation and reduction can be accomplished with hydrazine and hydrazine derivatives.
  • the tracers of the present invention are made by coupling a fluorescein moiety, or a derivative of fluorescein, to the general structure shown in Figures 2, 3 or 21 when Z is NH2, COOH, CN or OH.
  • the fluorescein moiety can be linked to the amino, carboxyl, imidate or alkoxy functional group by an amide, an amidine, a urea, a thiourea, a carbamate, a thiocarbonate, triazinylamino or sulfonylcarbamate linkage, as shown in Figure 11.
  • the fluorescein derivative is 6-carboxyfluorescein, and this is coupled to the precursor for 4-aminophencyclidine.
  • this reaction is performed in pyridine, but can also be perfomed in a co-solvent, e.g. , methanol, dimethylsulfoxide, or the like, in the presence of a base, e.g. , triethylamine or the like.
  • a co-solvent e.g. , methanol, dimethylsulfoxide, or the like
  • a base e.g. , triethylamine or the like.
  • the structure of the most preferred tracer is shown in Figure 14.
  • Useable tracers can be prepared from a variety of phencyclidine derivatives.
  • All phencyclidine derivatives that have a terminal amino group are coupled to carboxyfluorescein by the active ester method or the mixed anhydride method, preferably the active ester method, and coupled to fluorescein isothiocyanate, DTAF or alkoxy DTAF by simply mixing the two materials in solution.
  • the amino group can be converted to the isocyanate and thioisocyanate groups by reaction with phosgene and thiophosgene, respectively. These are then condensed with aminofluorescein to produce the tracer.
  • phencyclidine derivatives that have a terminal carboxylic acid group, such as carboxylic acid, (aminohydroxy)alkylcarboxylic acid or the like, are coupled to aminofluorescein by the active ester method.
  • All phencyclidine derivatives that have a terminal hydroxy group can be coupled to fluorescein by reaction with DTAF, iodoacetamidofluorescein or fluorescein isothiocyanate in solution.
  • the hydroxy group can be converted to the chlorosulfonylcarbamoyl, chloroformate and chlorothioformate groups by reaction with chlorosulfonylisocyanate, phosgene and thiophosgene, respectively.
  • These derivatives are then coupled to aminofluorescein or aminomethylfluorescein in solution to produce the tracer.
  • phencyclidine derivatives that have a terminal nitrile group are converted to imidates in anhydrous alcohol in the presence of hydrogen chloride gas.
  • the imidate is then coupled to fluorescein amine or aminomethylfluorescein in solution to prepare the tracer.
  • the particular tracer and antibodies of the present invention have been found to produce surprisingly good results in fluorescence polarization assays for phencyclidine and phencyclidine metabolites.
  • the assay of the present invention provides a more rapid phencyclidine and phencyclidine metabolite assay method than most prior art methods, because it requires no specimen treatment before analysis.
  • the assay system accurately measures the presence or quantity of phencyclidine and phencyclidine metabolites in a sample, because antibody specificity precludes detection of compounds other than phencyclidine-like compounds.
  • novel process of the present invention for determining the presence or amount of phencyclidine and phencyclidine metabolites in a sample comprises the steps of:
  • the most preferred form of the process of the present invention employs monoclonal antibodies prepared against an immunogen having the structure shown in Figure 23 with a tracer having the structure shown in Figure 14.
  • a sample containing, or suspected of containing, phencyclidine and/or phencyclidine metabolites is mixed with: (1) a biologically acceptable salt of a tracer; and (2) a monoclonal or polyclonal, preferably monoclonal, antibody specific to phencyclidine and phencyclidine metabolites and to the tracer.
  • the antibody is produced using the immunogen as described above.
  • the phencyclidine and phencyclidine metabolites and tracer compete for limited antibody sites, resulting in the formation of complexes.
  • the ratio of phencyclidine- and phencyclidine metabolites-antibody complex to tracer-antibody complex that is formed is directly proportional to the amount of phencyclidine and phencyclidine metabolites in the sample.
  • the results can be quantified in terms of net millipolarization units and span (in millipolarization units).
  • the measurement of net millipolarization units indicates the maximum polarization when a maximum amount of the tracer is bound to the antibody, in the absence of any phencyclidine or phencyclidine metabolites. The higher the net millipolarization units, the better the binding of the tracer to the antibody.
  • the assay span is the difference between the net millipolarization values obtained when the maximum amount of tracer is bound in the absence of any phencyclidine and the net millipolarization obtained when a specific amount of phencyclidine or phencyclidine metabolites is present in the sample.
  • a larger span allows for more millipolarization units to be placed between each of the calibrators of the standard curve generated for the assay, thereby providing better assay precision which, in turn, results in a better numerical analysis of the data obtained.
  • the most preferred antibody-tracer combination has a span of at least 90 millipolarization units, but smaller spans may be used to produce acceptable assays. It is important to note that the span varies depending on the sample size used which, in turn, may alter the preferred combination.
  • Table I shows the results obtained with various embodiments of the tracers, antibodies and assay of the present invention, in terms of span and net millipolarization units at a sample size of 2 uL when the sample contains 75 ng/mL of phencyclidine.
  • an assay produced from an immunogen made from the hapten of Figure 18 used in combination with the tracer of Figure 13 and a 2 uL sample size provides good results. Accordingly, this combination of antibody and tracer is a preferred form of the invention for a sample size of 2 uL.
  • the most preferred form of the assay of the present invention employs monoclonal antibodies prepared against an immunogen having the structure shown in Figure 23 with tracers having the structure shown in Figure 14.
  • the antibody/tracer combinations represented by the combinations of Figures 18 and 12, Figures 18 and 14, Figures 18 and 15, and Figures 18 and 16 also produced acceptable results and are alternative preferred combinations.
  • Table II demonstrates the specificity of the monoclonal antibodies produced against an immunogen having the structure shown in Figure 23 when compared with polyclonal antibodies of sheep and rabbits raised against the same immunogen. Crossreactivity to a panel of 10 different compounds was examined using antisera from sheep and rabbits and mouse monoclonal antibodies, all of which were raised against an immunogen having the structure shown in Figure 23 and tested with the tracer of Figure 14.
  • the pH at which the method of the present invention is practiced must be sufficient to allow the fluorescein moiety of the tracers to exist in their open form.
  • the pH may range from about 3 to 12, more usually in the range of from about 5 to 10, most preferably from about 6 to 9.
  • Various buffers may be used to achieve and maintain the pH during the assay procedure. Representative buffers include borate, phosphate, carbonate, tris, barbital and the like. The particular buffer employed is not critical to the present invention, but the tris and phosphate buffers are preferred.
  • the cation portion of the buffer will generally determine the cation portion of the tracer salt in solution.
  • Riboflavin binding protein is added to the sample or to one or more of the assay reagents in order to bind any riboflavin present in the sample into RBP-riboflavin complexes, thus eliminating potential fluorescence interference.
  • RBP is a protein of approximately 32,000 M.W. which is isolated from egg whites. Upon isolation from the egg, each molecule of RBP contains one molecule of riboflavin. This, the holoprotein form of RBP, must be converted to the apoprotein form by dialysis, under acidic conditions, to remove the bound riboflavin.
  • the RBP apoprotein utilized in the present invention is commercially available from Sigma Chemical Company, St. Louis, Missouri. The amount used is not critical, provided a sufficient quantity is used to bind all free riboflavin in the sample.
  • phencyclidine and phencyclidine metabolites have a tendency to adhere to the plastic components of instrument probes. This results in the carryover of phencyclidine and phencyclidine metabolites from one sample to other samples.
  • Standard dilution buffer which contains 0.1 M sodium phosphate, 0.01% bovine gamma globulin and 0.1% sodium azide, pH 7.5, is not sufficient to remove the phencyclidine and phencyclidine metabolites from the probe.
  • the assay is a "homogeneous assay," which means that the end polarization readings are taken from a solution in which bound tracer is not separated from unbound tracer. This is a distinct advantage over heterogeneous immunoassay procedures, such as those where the bound tracer must be separated from the unbound tracer before a reading can be taken.
  • the reagents for the fluorescence polarization assay of the present invention comprise: (1) monoclonal or polyclonal antibodies for phencyclidine and phencyclidine metabolites; and (2) tracer reagent.
  • Monoclonal antibodies are the preferred antibodies for use in the assay of the present invention.
  • the most preferred antibodies for use in this assay are monoclonal antibodies generated against an immunogen having the structure shown in Figure 23.
  • Typical solutions of these reagents are commercially available in assay "kits” from Abbott Laboratories, Abbott Park, Illinois.
  • the tracer formulation presently preferred is 164 nanomolar tracer in: 0.1 molar tris buffer at pH 7.9; 10% sodium cholate; 0.1% sodium azide; and 0.01% bovine gamma-globulin.
  • the antiserum formulation comprises mouse monoclonal antibody diluted with: 0.05 molar HEPES buffer at pH 7.5; 0.1% sodium azide; 1.0% ovalbumin; and 10% glycerol (volume/volume).
  • the dilution buffer comprises: 0.1 molar sodium phosphate at pH 7.5; 0.1% sodium azide; and 0.01% bovine gamma-globulin.
  • the pretreatment solution comprises: 0.01% bovine gamma-globulin; 0.1 molar tris buffer at pH 7.5; 0.1% sodium azide; and 10mg/mL riboflavin binding protein.
  • Phencyclidine calibrators comprising phencyclidine in normal human urine at concentrations of 0.0, 25.0, 60.0, 120.0, 250.0, and 500.0 nanograms per milliliter, with 0.1% sodium azide as a preservative are useful.
  • Phencyclidine controls comprising phencyclidine in normal human urine are provided at concentrations of 35.0, 100.0 and 250.0 nanograms per milliliter with 0.1% sodium azide as a preservative are also useful.
  • the preferred procedure is especially designed to be used in conjunction with the Abbott TD x ® Clinical Analyzer or the Abbott AD x ® Drugs of Abuse System, both of which are available from Abbott Laboratories, Abbott Park, Illinois. Fifty microliters of urine is required. The calibrators, controls, or unknown samples are pipetted directly into the sample well of the TD x ® sample cartridge.
  • One of the advantages of this procedure is that the sample does not require any special preparation. The assay procedure from this point is fully automated.
  • the sample is mixed with the pretreatment solution in dilution buffer and a background reading is taken.
  • the tracer is then mixed with the assay.
  • the antibody is then finally mixed into the test solution. After incubation, a fluorescence polarization reading is taken.
  • the fluorescence polarization value of each calibrator, control or sample is determined and is printed on the output tape of an instrument, such as the Abbott TD x ® Analyzer or AD x ® System.
  • a standard curve is generated in the instrument by plotting the polarization of each calibrator versus its concentration using a nonlinear regression analysis.
  • the concentration of each control or sample is read off of the stored calibration curve and printed on the output tape.
  • the tracer, antibody, pretreatment solution, wash solution, calibrators and controls should be stored between about 2°C and about 8°C while the dilution buffer should be stored at ambient temperature.
  • a standard curve and controls should be run every two weeks, with each calibrator and control run in duplicate. All samples can be run in duplicate.
  • a significant feature of the most preferred assay of the present invention one which employs a monoclonal antibody prepared against an immunogen having the structure shown in Figure 23 and a tracer having the structure shown in Figure 14, is the high degree of specificity to phencyclidine, phencyclidine metabolites and phencyclidine analogs, while greatly minimizing crossreactivity to a host of other synthetic and naturally-occuring compounds.
  • Representative crossreactivity data for phencyclidine metabolites and phencyclidine analogs employing the assay of the present invention wherein the tracer has the structure shown in Figure 14 and the antibodies have been raised against an immunogen having the structure shown in Figure 23 are shown in Table 3(a) below. The four columns indicate the following information:
  • Another advantage of the assay of the present invention is the low cross-reactivity of the assay with nonphencyclidine compounds.
  • Representative cross-reactivity data which indicate a low cross-reactivity of the assay for compounds which have a similar chemical structure to phencyclidine are shown in Table 3(b) (for a tracer having the structure shown in Figure 14 and monoclonal antibodies generated against an immunogen having the structure shown in Figure 23).
  • the four columns in Table 3(b) indicate the same information as is described above for Table 3(a).
  • the assay of the present invention was also compared to other methods for the detection of phencyclidine, such as gas chromatography/mass spectrometry (GC/MS), radioimmunoassay (RIA) and enzyme multiplied immunoassay technology (EMIT) by testing drug-free urine specimens and urine specimens containing phencyclidine and phencyclidine metabolites with each of these methods.
  • GC/MS gas chromatography/mass spectrometry
  • RIA radioimmunoassay
  • EMIT enzyme multiplied immunoassay technology
  • Examples I through III and XVII are directed to preparation of an immunogen useful for producing antibody; Examples IV through IX, XI and XII are directed to the synthesis of precursors for immunogens and tracers; Examples X and XIII through XVI are directed to the preparation of tracers; and Example XVIII describes an experiment during which monoclonal antibodies were prepared against an immunogen having the structure shown in Figure 23.
  • 1-benzylpiperazine (Aldrich Chemical Co., Inc., supra) (6.12g) was dissolved in 10 mL deionized water and cooled to 0°C. Concentrated hydrochloric acid (3.6 mL) was added to adjust the pH to 5. After warming to room temperature, 3.6 mL cyclohexanone was added, followed by potassium cyanide (2.4 g) in 6 mL deionized water. The solution slowly became cloudy. After 18 hours, the solid was filtered. The solid was dissolved in chloroform, dried over Na2SO4, filtered and the solvent was removed in vacuo to yield pure 1-benzyl-4-(1-cyanocyclohexyl) piperazine.
  • 1-benzyl-4-(1-phenylcyclohexyl)piperazine (0.47 g) was dissolved in 86 mL methanol and 14 mL 0.2 N HCl in methanol. The mixture was hydrogenated over palladium black (0.1175 g) and 3 atm. of hydrogen at room temperature for 1 hour. The reaction was filtered and the solvent was removed in vacuo . The residue was chromatographed on silica gel eluted with the appropriate mixture of methanol and chloroform to yield pure 1-(1-phenylcyclohexyl)piperazine.
  • 4-hydroxypiperidine (Aldrich Chemical Co., Inc., supra) was dissolved in distilled water (14 mL), cooled to 0°C and the pH was adjusted to between 4 and 5 by addition of concentrated hydrochloric acid and 4-hydroxypiperidine. After warming to room temperature, 5.2 mL cyclohexanone and 3.3 g potassium cyanide in water (9 mL) were added sequentially. After 18 hours of stirring at room temperature, the solid was filtered. The solid was dissolved in 100 mL methylene chloride, dried over Na2SO4, filtered and the solvent was removed in vacuo to yield pure 1-(1-cyanocyclohexyl)-4-hydroxypiperidine.
  • 1-(1-phenylcyclohexyl)-4-hydroxypiperidine (0.261 mg) was suspended in 5 mL dry benzene and 2 mL 10% phosgene in benzene was added. After stirring, and then stoppering for 3 hours at room temperature, 1 mL of chloroform was added. After 30 minutes, the solvent was removed in vacuo . Carbon tetrachloride (dry) (1mL) was added and removed in vacuo to yield 4-(1-(1-phenyl cyclohexyl))piperidinyl chloroformate as a white solid.
  • 1-(1-phenylcyclohexyl)-4-hydroxypiperidine was dissolved in 15 mL glacial acetic acid and 0.3 mL concentrated slufuric acid, and 1.9 mL Jones reagent (made from 26.72 g H2CrO4 and 23 mL H2SO4 diluted to 100 mL with water) was added dropwise.
  • Example XIII The same procedure was used as in Example XIII except that 6-((4,6-dichloro-1,3,5-triazin-2-yl)amino) fluorescein was used instead of 5-((4,6-dichloro-1,3,5-triazin-2-yl)amino)fluorescein.
  • 6-carboxyfluorescein (Calbiochem, La Jolla, CA) (14 mg), N-hydroxy succinimide (6 mg) and N,N'-dicyclohexyl-carbodiimide (14 mg) were dissolved in 0.5 mL dry pyridine and stirred at room temperature, and then stoppered. After 1 hour, 4-amino-1-(1-phenylcyclohexyl) piperidine (9 mg) was added followed by 0.5 mL dry pyridine. After 15 hours, the reaction was chromatographed on silica gel preparative plates eluted with the appropriate mixture of methanol, chloroform and acetic acid.
  • Example XV The same procedure was used as in Example XV except that 5-carboxyfluorescein (Calbiochem, supra) was used instead of 6-carboxyfluorescein.
  • the mixture was stirred overnight at room temperature and subsequently dialyzed against 60% DMSO for 8 hours. During the following dialysis, the DMSO was reduced to 25%. The final three dialysis changes were 0.05 M sodium phosphate buffer at pH 7.5. The resulting fluffy white precipitate was removed from the dialysis bag and harvested by centrifugation. The pellet containing the precipitate was resuspended in a minimum amount of buffer and used as the immunogen in Example XVIII.
  • mice Six week old female BALB/c mice were immunized intraperitoneally with 100 ug of an immunogen having the structure shown in Figure 23 mixed 1:1 in RIBI adjuvant (RIBI Immunochem, Hamilton, Montana) into two different sites in the ventral rear peritoneal cavities during weeks 1, 5, 9 and 16.
  • RIBI adjuvant RIBI Immunochem, Hamilton, Montana
  • a competitive binding immunoassay is run by adding free phencyclidine to the sample.
  • the free phencyclidine will compete with the tracer for the binding sites on the antibody. If the free phencyclidine binds to the antibody, this indicates that the antibody is specific for phencyclidine and this will prevent the tracer from binding to the antibody.
  • the total signal (amount of fluorescence read by an instrument, such as the Abbott TD x ® Analyzer) will be less.
  • mice Serum samples were taken from the mice two weeks after each immunization and then analyzed on an Abbott Laboratories' TD x ® Clinical Analyzer, available from Abbott Laboratories, Abbott Park, Illinois, and on a Pandex Screen Machine (Baxter Healthcare Corporation, Mundelein, Illinois). After the fourth immunization and subsequent analysis of serum samples, four mice were chosen for use in the fusion of B-lymphocyte cells with myeloma cells. Each of these mice had been found to be producing antibodies specific for phencyclidine and phencyclidine metabolites based upon 50% displacement of total signal using 500 ng/mL of free phencyclidine in a competitive binding immunoassay with a tracer compound having the structure shown in Figure 14.
  • B-lymphocyte cells were then removed from the mouse by standard procedures. Generally, the mouse was sacrificed, doused with 70% EtOH, and then the spleen was asceptically removed with sterile instruments. The spleen was washed in IMDM (Iscove's Modified Dulbecco's Medium) with 1% pen-strep and 1% L-glutamine and transferred to a petri dish. Using a 23 g needle on a 12 mL syringe, 20 holes were punctured into the spleen.
  • IMDM Iscove's Modified Dulbecco's Medium
  • the B-lymphocyte cells were flushed out of the spleen with two injections of 10 mL of IMDM with 1% pen-strep and 1% L-glutamine. Using a cell scraper, the spleen was gently pressed while the B-lymphocyte cells were continuously flushed out until the spleen appeared translucent. The resulting B-lymphocyte cell suspension was then filtered through Nytex filters (Tetko, Elmsford, New York) into a 50 mL centrifuge tube. The B-lymphocyte cell suspension was then centrifuged for 5 minutes at 1000 rpm.
  • the supernate was aspirated off, and the B-lymphocyte cell suspension was resuspended in 10 mL of IMDM with 1% pen-strep and 1% L-glutamine.
  • the cells were then counted using a hemocytometer to obtain the concentration of cells per mL of IMDM with 1% pen-strep and 1% L-glutamine.
  • Myeloma cells to be used in the production of hybridomas may be obtained from the American Type Culture Collection, Rockville, Maryland. They must be in a healthy log phase with viability of greater than 95%. The most desirable myelomas are those of low passage number (those obtained from a fresh stock). In addition, in a fusion of myeloma cells with B-lymphocyte cells, the number of myeloma cells should preferably be in a one to one ratio with the number of B-lymphocyte cells.
  • SP2/0 myeloma cells were centrifuged for 5 minutes at 1000 rpm. After the supernate was decanted from the centrifuge tube, the B-lymphocyte cells described above were fused with SP2/0 myeloma cells in a 2:1 ratio of B-lymphocyte cells to myeloma cells using the procedures described in Kohler and Milstein, supra , with the exception that a PEG 1450 solution, MW 1300-1600 (polyethylene glycol, American Type Culture Collection, Rockville, MD), rather than sendai virus, was employed to fuse the myeloma cells to the B-lymphocyte cells.
  • a PEG 1450 solution MW 1300-1600 (polyethylene glycol, American Type Culture Collection, Rockville, MD), rather than sendai virus
  • the pellet of myeloma cells which resulted after centrifugation was resuspended with the above-described B-lymphocyte cell suspension, and then the resulting suspension was centrifuged for 5 minutes at 1000 rpm. The supernate was then aspirated from the centrifuge tube, leaving a very dry pellet. The pellet was loosened by gently tapping the bottom of the centrifuge tube on a hard object and 1 mL of a PEG 1450 solution (prepared by diluting 1 mL of PEG 1450 solution with 2 mL of IMDM with 1% pen-strep and 1% L-glutamine) was slowly added to the loosened pellet for about 10 seconds.
  • a PEG 1450 solution prepared by diluting 1 mL of PEG 1450 solution with 2 mL of IMDM with 1% pen-strep and 1% L-glutamine
  • the centrifuge tube was then rotated to ensure the even distribution of the PEG solution throughout the cell mixture for about 20 seconds.
  • the resulting fusion mixture was then slowly resuspended with 10 mL IMDM with 1% pen-strep and 1% L-glutamine and then centrifuged for 5 minutes at 1000 rpm.
  • HAT selective IMDM [IMDM plus 1% 1-glutamine, 1% pen-strep, 1% HAT media (Gibco, Grand Island, New York) and 10% fetal bovine serum (Hyclone, Logan, Utah)] and then plated out at a concentration of 3 x 105 cells per well in HAT selective IMDM in 96-well tissue culture plates (Nunc, Naperville, Illinois). STM mitogen (RIBI Immunochem, Hamilton, Montana) was added to the initial plating media in order to promote hybrid survival.
  • Hybrid colonies which resulted were fed with HT media [IMDM plus 1% 1-glutamine, 1% penn-strep, 1% HT (Gibco, Grand Island, New York) and 10% fetal bovine serum (Hyclone, Logan, Utah)] on days 5 and 7 post fusion.
  • HT media IMDM plus 1% 1-glutamine, 1% penn-strep, 1% HT (Gibco, Grand Island, New York) and 10% fetal bovine serum (Hyclone, Logan, Utah)
  • the cloning of the hybrids was performed by limiting dilution in HT media. Generally, the following dilutions of hybrids were prepared using HT media:
  • Clone selection was based on the ability of the antibodies produced by the clones to: (1) displace the tracer described above with 500 ng/mL of free phencyclidine (greater than 80% displacement); and (2) not be inhibited by the initial cross reactivity panel of 10 different compounds (greater than 50% with respect to each of amitriptyline, nortriptyline, imipramine, desipramine, dextromethorphan, levallorphan, promazine, ketamine, orphenadrine, diphenhydramine, each of which was tested at 100 ug/mL in PBS).
  • hybridoma cell lines BALB/c mouse B-lymphocyte-SP2/O myeloma fusion cell lines
  • clone cell lines was designated PCP 2-101-189, was deposited on May 16, 1990, with the American Type Culture Collection (ATCC), Rockville, Maryland, USA, and was given accession number HB10456 by the ATCC.

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WO1993012111A1 (en) * 1991-12-16 1993-06-24 Biosite Diagnostics Incorporated Novel cocaine derivatives and protein and polypeptide cocaine derivative conjugates and labels
WO1993020049A1 (en) * 1992-04-06 1993-10-14 Biosite Diagnostics Incorporated Novel phencyclidine derivatives and protein and polypeptide phencyclidine derivative conjugates and labels
EP0747707A1 (de) * 1995-05-19 1996-12-11 F. Hoffmann-La Roche Ag Propoxyphenderivate als Immunoassay-Reagenzien
EP0816364A1 (de) * 1996-07-02 1998-01-07 F. Hoffmann-La Roche Ag Reagenzien für einen Lysersäure Diethylamid Immuntest
US6242463B1 (en) 1994-10-31 2001-06-05 Opt-E-Scrip, Inc. Method and kit for treating illnesses
DE10112198A1 (de) * 2001-03-14 2002-09-19 Gruenenthal Gmbh Substituierte Dimethyl-[1-(1-phenyl-cyclohexyl)-piperidin-3-ylmethyl]-amine
EP1333023A1 (de) * 2002-01-31 2003-08-06 Randox Laboratories Ltd. Haptene, Immunogene, Antikörper und Konjugate für Ketamin und dessen Metaboliten
CN102627696A (zh) * 2012-04-11 2012-08-08 杭州培乐生物技术有限公司 一种苯环利定人工抗原的制备方法
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AU2311599A (en) * 1998-03-28 1999-10-18 Vladimir V Martin Amplified fluorescent materials and uses thereof
US6809249B2 (en) * 2001-01-12 2004-10-26 Protune Corp. Self-aligning ultrasonic displacement sensor system, apparatus and method for detecting surface vibrations
US8962677B2 (en) * 2007-07-12 2015-02-24 Acumen Pharmaceuticals, Inc. Methods of restoring cognitive ability using non-peptidic compounds
US9006283B2 (en) * 2007-07-12 2015-04-14 Acumen Pharmaceuticals, Inc. Methods of modifying amyloid β oligomers using non-peptidic compounds
US20110098309A1 (en) * 2007-07-12 2011-04-28 Acumen Pharmaceuticals, Inc. Methods of inhibiting the formation of amyloid-beta diffusable ligands using acylhydrazide compounds
WO2009079566A2 (en) 2007-12-18 2009-06-25 Acumen Pharmaceuticals, Inc. Novel addl receptor polypeptides, polynucleotides and host cells for recombinant production
JP6355289B1 (ja) * 2017-12-01 2018-07-11 株式会社奥本研究所 有機エレクトロルミネッセンス素子
CN113151188B (zh) * 2021-04-27 2022-10-18 江南大学 一株分泌苯海拉明单克隆抗体的杂交瘤细胞株及其应用

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EP0218010A2 (de) * 1985-07-10 1987-04-15 Abbott Laboratories Verfahren zur Bestimmung von Liganden und substituierte Carboxyfluoreszein-Markers zur Durchführung desselben

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Publication number Priority date Publication date Assignee Title
WO1993012111A1 (en) * 1991-12-16 1993-06-24 Biosite Diagnostics Incorporated Novel cocaine derivatives and protein and polypeptide cocaine derivative conjugates and labels
WO1993020049A1 (en) * 1992-04-06 1993-10-14 Biosite Diagnostics Incorporated Novel phencyclidine derivatives and protein and polypeptide phencyclidine derivative conjugates and labels
US6242463B1 (en) 1994-10-31 2001-06-05 Opt-E-Scrip, Inc. Method and kit for treating illnesses
US6579888B2 (en) 1994-10-31 2003-06-17 Opt-E-Scrip, Inc. Method and kit for treating illnesses
EP0747707A1 (de) * 1995-05-19 1996-12-11 F. Hoffmann-La Roche Ag Propoxyphenderivate als Immunoassay-Reagenzien
US5817529A (en) * 1995-05-19 1998-10-06 Roche Diagnostic Systems, Inc. Methods of making propoxphene derivatives
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EP0816364A1 (de) * 1996-07-02 1998-01-07 F. Hoffmann-La Roche Ag Reagenzien für einen Lysersäure Diethylamid Immuntest
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US7049327B2 (en) 2001-03-14 2006-05-23 Gruenenthal Gmbh Substituted dimethyl-[1-(1-phenyl-cyclohexyl)-piperidin-3-ylmethyl]-amines and the use of the same as analgesics
DE10112198A1 (de) * 2001-03-14 2002-09-19 Gruenenthal Gmbh Substituierte Dimethyl-[1-(1-phenyl-cyclohexyl)-piperidin-3-ylmethyl]-amine
EP1333023A1 (de) * 2002-01-31 2003-08-06 Randox Laboratories Ltd. Haptene, Immunogene, Antikörper und Konjugate für Ketamin und dessen Metaboliten
US7371829B2 (en) 2002-01-31 2008-05-13 Randox Laboratories Limited Haptens, immunogens, antibodies and conjugates to ketamine and its metabolites
CN102627696A (zh) * 2012-04-11 2012-08-08 杭州培乐生物技术有限公司 一种苯环利定人工抗原的制备方法
CN102627696B (zh) * 2012-04-11 2013-09-25 杭州博林生物技术有限公司 一种苯环利定人工抗原的制备方法
US10195153B2 (en) 2013-08-12 2019-02-05 Pharmaceutical Manufacturing Research Services, Inc. Extruded immediate release abuse deterrent pill
US10639281B2 (en) 2013-08-12 2020-05-05 Pharmaceutical Manufacturing Research Services, Inc. Extruded immediate release abuse deterrent pill
US9492444B2 (en) 2013-12-17 2016-11-15 Pharmaceutical Manufacturing Research Services, Inc. Extruded extended release abuse deterrent pill
US10172797B2 (en) 2013-12-17 2019-01-08 Pharmaceutical Manufacturing Research Services, Inc. Extruded extended release abuse deterrent pill
US10792254B2 (en) 2013-12-17 2020-10-06 Pharmaceutical Manufacturing Research Services, Inc. Extruded extended release abuse deterrent pill
US9707184B2 (en) 2014-07-17 2017-07-18 Pharmaceutical Manufacturing Research Services, Inc. Immediate release abuse deterrent liquid fill dosage form
US10959958B2 (en) 2014-10-20 2021-03-30 Pharmaceutical Manufacturing Research Services, Inc. Extended release abuse deterrent liquid fill dosage form

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KR910020036A (ko) 1991-12-19
JPH04235199A (ja) 1992-08-24
DE69113114D1 (de) 1995-10-26
US5407834A (en) 1995-04-18
EP0459387B1 (de) 1995-09-20
DE69113114T2 (de) 1996-05-02
EP0459387A3 (en) 1992-09-02
CA2043372A1 (en) 1991-11-30
ATE128241T1 (de) 1995-10-15
US5155212A (en) 1992-10-13
AU643524B2 (en) 1993-11-18
ES2080188T3 (es) 1996-02-01

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